Dong Siqi, Wang Zhangyang, Wang Qin, Huang Zhen, Dong Jihong, Wu Shuai
Department of Neurology, Zhongshan Hospital, Fudan University, Shanghai 200032, P.R. China.
Exp Ther Med. 2025 Aug 13;30(4):197. doi: 10.3892/etm.2025.12947. eCollection 2025 Oct.
Immune checkpoint inhibitors (ICIs) play a crucial role in cancer therapy by enhancing anti-tumor immune responses. However, they may also induce immune-related adverse events (irAEs) such as polyradiculoneuropathy (PRN) and cardiomyopathy, which, although rare, can be life-threatening. Traditional treatments, including corticosteroids and intravenous immunoglobulin (IVIG), often show limited efficacy, underscoring the need for alternative therapeutic strategies. The present study reported the case of a 63-year-old female diagnosed with pancreatic ductal adenocarcinoma who developed profound neurological and cardiac dysfunction, including bilateral ptosis, limb weakness and dysphagia, following chemotherapy and ICI therapy. Initial immunotherapy with IVIG and corticosteroids resulted in only partial clinical improvement. Subsequent administration of efgartigimod induced significant neurological recovery, with normalization of both the Inflammatory Neuropathy Cause and Treatment disability score and Activities of Daily Living scale following four weekly doses. Clinical improvement was accompanied by reductions in both cytokine and immunoglobulin levels. This case illustrates the therapeutic potential of efgartigimod in managing ICI-induced PRN and cardiomyopathy, particularly in patients refractory to standard therapies. The observed improvements suggest that antibody-mediated pathways may play a pivotal role in the pathogenesis of irAEs. Further studies are warranted to confirm the efficacy and safety of efgartigimod in alleviating ICI-related irAEs in broader clinical settings.
免疫检查点抑制剂(ICIs)通过增强抗肿瘤免疫反应在癌症治疗中发挥关键作用。然而,它们也可能诱发免疫相关不良事件(irAEs),如多神经根神经病(PRN)和心肌病,尽管罕见,但可能危及生命。包括皮质类固醇和静脉注射免疫球蛋白(IVIG)在内的传统治疗方法往往疗效有限,这凸显了对替代治疗策略的需求。本研究报告了一例63岁女性,被诊断为胰腺导管腺癌,在化疗和ICI治疗后出现严重的神经和心脏功能障碍,包括双侧上睑下垂、肢体无力和吞咽困难。最初使用IVIG和皮质类固醇进行免疫治疗仅使临床症状部分改善。随后给予艾加莫德后,神经功能显著恢复,在每周一次的四次给药后,炎症性神经病病因及治疗残疾评分和日常生活活动量表均恢复正常。临床症状的改善伴随着细胞因子和免疫球蛋白水平的降低。该病例说明了艾加莫德在治疗ICI诱导的PRN和心肌病方面的治疗潜力,特别是在对标准治疗无效的患者中。观察到的改善表明,抗体介导的途径可能在irAEs的发病机制中起关键作用。有必要进行进一步研究,以确认艾加莫德在更广泛临床环境中缓解ICI相关irAEs的疗效和安全性。